助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   还原酶基因 的翻译结果: 查询用时:0.035秒
图标索引 在分类学科中查询
所有学科
内分泌腺及全身性疾病
更多类别查询

图标索引 历史查询
 

还原酶基因
相关语句
  reductase gene
     Identification of a compound heterozygote Arg57 Gln/Cys203Tyr in NADH-cytochrome b5 reductase gene
     NADH-细胞色素b5还原酶基因Arg57Gln/Cys203Tyr复合杂合子鉴定
短句来源
     Detection of N~5,N~ 10-methylenetetrahydrofolate reductase gene polymorphism by using PCR-RFLP and its clinical significance
     PCR-RFLP法检测N~5,N~(10)-亚甲基四氢叶酸还原酶基因多态性及其临床意义
短句来源
     Expression of Pichia stipitis Xylose Reductase Gene XYL1 in Saccharomyces cerevisiae
     木糖发酵酵母Pichia stipitis木糖还原酶基因XYL1在酿酒酵母中的表达
短句来源
     Relationship between polymorphisms in methylenetetrahydrofolate reductase gene 1298AC and H. pylori infection in gastric cancer
     胃癌亚甲基四氢叶酸还原酶基因1298AC多态性与H.pylori感染的关系
短句来源
     C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion
     原因不明复发性流产患者血中亚甲基四氢叶酸还原酶基因C677T和A1298C位点突变的研究
短句来源
更多       
  reductase genes
     Cotransduction of Human mdr-1 and Dihydrofolate Reductase Genes into Murine Hematopoietic Cells
     人多药耐药基因-1及二氢叶酸还原酶基因共转导小鼠造血细胞
短句来源
     Relationships between polymorphisms of angiotensin-converting enzyme and methylenete-trahydrofolate reductase genes and genetic susceptibility to pregnancy induced hypertension
     血管紧张素I转换酶基因和N~5,N~(10)-亚甲基四氢叶酸还原酶基因多态性与妊娠高血压综合征发病的关系
短句来源
     Sequence alignment showed that orfA had a high homology of nucleotide acid composition to monooxygenase genes from both Japonicum USDA 110 and Ralstonia eutropha HF 39, orfB had some homology to the component of flavin reductase genes from Bordetlla pertussis Tohama I, Ralstonia solanacearum GMI1000 and Bordetella bronchiseptica RB50.Enzyme activity analysis showed that the cell extracts of recombinant E.
     序列比对发现,orfA序列与JaponicumUSDA110和RalstoniaeutrophaHF39中的加单氧酶基因同源性较高,orfB序列与BordetllapertussisTohamaI、RalstoniasolanacearumGMI1000和BordetellabronchisepticaRB50等菌中的黄素还原酶基因有一定的同源性。
短句来源
     Two rice arsenate reductase genes (OsACR2s) have been cloned and characterized recently.
     最近,水稻砷酸盐还原酶基因已经被克隆和表征。
短句来源
  “还原酶基因”译为未确定词的双语例句
     A Statistical Study on the Relationship between Gene Polymorphisms of β-fibrinogen 148C/T,N5,N10-methylene-tetra-hydrofolic Acid Reductase 677C/T and Cerebral Infarction
     纤维蛋白原β基因148C/T及亚甲基四氢叶酸还原酶基因677C/T多态性与脑梗死的关系研究
短句来源
     The relationship between C677T mutation of 5,10-methylenetetrahydrofolate reductase and recurrent cerebral infarction
     5,10-亚甲基四氢叶酸还原酶基因C677T突变与再发脑梗死的关系
短句来源
     A case-control study on the polymorphisms of methylenetetrahydrofolate reductase 1298A→C and susceptibility of esophageal cancer
     亚甲基四氢叶酸还原酶基因1298A→C多态与食管癌易感性关系的病例对照研究
短句来源
     Transformation and Function Analysis of a Steroid 5 Alpha-Reductase Gene (GhDET2) in Cotton (Gossypium Hirsutum L.)
     棉花类固醇5a-还原酶基因(GhDET2)的遗传转化及其功能分析
短句来源
     Structure Genes dhaB (4.6kb) and dhaT (1.16kb) encoding essential enzymes of 1,3-propanediol pathway were amplified by PCR technique using Klebsiella pneumoniae 1192-121# chromosomal DNA as a template. And the primers design refered to the sequence of Klebsiella pneumoniae ATCC 25955 publicated by NCBI. dhaB and dhaT were inserted into the downstream of tac promoter.
     利用PCR技术,以肺炎克雷伯氏菌(Klebsiella pneumoniae)1192-121#基因组DNA为模板,以NCBI报道的Klebsiella pneumoniae ATCC 25955相关基因序列为参考设计引物,扩增出约4.6kb的编码甘油脱水酶基因dhaB和1.16kb的编码1,3-丙二醇氧化还原酶基因dhaT。
短句来源
更多       
查询“还原酶基因”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  reductase gene
Differential Regulation of Nitrate Reductase Gene Expression in Corn Cockle Embryos by Cytokinin and Nitrate
      
The full sequence of the nitrate reductase gene was obtained from a type isolate of Verticillium fungicola var.
      
Frequencies of C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene at the early stage of human developmen
      
A cDNA fragment of the ferric chelate reductase gene (FRO1) from tomato was inserted into the DNAmβ vector.
      
C677T mutation from methylenetetrahydrofolate reductase gene (MTHFR) was chosen as model samples to assess the feasibility of this method.
      
更多          
  reductase genes
Localization of NAD(P)H-bispecific nitrate reductase genes to chromosomes of barley, rye, wheat and Aegilops umbellulata
      
In addition, a gene (grdX) encoding a 13.7-kDa protein of unknown function seemed to be associated with the reductase genes.
      
Based on sequence analysis of the 16S rRNA gene and the sulfite reductase genes dsrAB, strain FiPS-3 was found to be closely related to Desulfotignum balticum.
      
AkMO and EaCoMT genes were found in a putative operon that included CoA transferase, acyl-CoA synthetase, dehydrogenase, and reductase genes.
      
In summary, mutations in the WT1, AR and 5α-reductase genes are not common causes of isolated hypospadias.
      
更多          
  chelate reductase gene
A cDNA fragment of the ferric chelate reductase gene (FRO1) from tomato was inserted into the DNAmβ vector.
      
Molecular and phenotypic characterization of transgenic soybean expressing the Arabidopsis ferric chelate reductase gene, FRO2
      
Here we demonstrate that heterologous expression of the Arabidopsis thaliana ferric chelate reductase gene, FRO2, in transgenic soybean significantly enhances Fe+3 reduction in roots and leaves.
      
Isolation and characterization of Fe(III)-chelate reductase gene LeFRO1 in tomato
      


Southern blot analysis showed great homology existed between niaD (NR gene) of Aspergillus nidulans and A. mediterranei U-32 chromosome DNA. A 5.0 kb PstI fragment from A. mediterranei U-32 complementary to A. nidulans niaD gene was cloned in E. colt NM522 using niaD as a probe. An identical DNA band was observed through back-hybridization of the cloned DNA fragment to chromosome DNA of A. mediterranei U-32. Its 2.1kb Sma I -EcoR V fragment can only hybridize with total RNA from nitrate-cultured mycelium. These...

Southern blot analysis showed great homology existed between niaD (NR gene) of Aspergillus nidulans and A. mediterranei U-32 chromosome DNA. A 5.0 kb PstI fragment from A. mediterranei U-32 complementary to A. nidulans niaD gene was cloned in E. colt NM522 using niaD as a probe. An identical DNA band was observed through back-hybridization of the cloned DNA fragment to chromosome DNA of A. mediterranei U-32. Its 2.1kb Sma I -EcoR V fragment can only hybridize with total RNA from nitrate-cultured mycelium. These data suggested that the cloned DNA fragment contains NR gene of A. mediterranei U-32. This is the first report on NR gene cloning from aerobic bacteria. It was deduced from molecular weigh of NR that its gene sequence is about 1. 5kb in size. Further hybridization analysis indicated that the cloned DNA fragment covers the full-length NR gene of A. mediterranei U-32. We also constructed the physical map of the recombinant plasmid pJL1-with various restriction endonuclease, among them ten with no restriction site, six with unique site and two with double sites on the insert.

Southern杂交分析表明在地中海拟无枝菌酸菌U-32染色体DNA和黑曲霉niaD(硝酸还原酶基因)之间存在着明显的同源性。利用异源niaD探针从地中海拟无枝菌酸菌U-32基因文库中筛选得到一个能与niaD杂交的5.0kb的PstⅠ片段。该片段经同位素标记后能与地中海拟无枝菌酸菌U-32染色体上一个相同的PstⅠ片段杂交,位于这一片段上的2.1kb SmaⅠ-EcoR Ⅴ片段只能与以硝酸盐为唯一氮源的总RNA杂交,而不能与相同条件下以铵盐为唯一氮源的总RNA杂交,这些结果表明,所克隆到的5.0kb PstⅠDNA片段含有地中海拟无枝菌酸菌U-32的硝酸还原酶基因。这是好氧细菌硝酸还原酶基因克隆的首次报道。由该酶蛋白分子量推测,其结构基因大小在1.5kb左右,进一步的杂交分析发现在5.0kb的PstⅠ片段中含有完整的NR基因。用20种限制酶对重组质粒pJL1进行了限制酶酶谱的构建,发现有10种酶在pJL1外源片段上无切点,6种酶为单切点,EcoRⅠ与SmaⅠ各有两个切点。

This paper presents the results about the expression of the polyketide ke-toreductase gene (PKG) from midecamycin producing strain (S. mycarofaciens 1748), gene localization and nucleotide sequences analysis of the PKG.

将麦迪霉素产生菌基因文库中与放线紫红素酮基还原酶基因actⅢ有同源性的4.0kb DNA片段克隆到质粒载体pWHM3中,构成重组质粒pCB4。将质粒pCB4转入酮基还原酶基因缺陷菌株——加利利链霉菌ATCC31671中,得到转化子。转化子发酵产物经TLC和HPLC分析证明是阿克拉菌酮,与加利利链霉菌原株ATCC31133的产物相同,说明麦迪霉素产生菌酮基还原酶基因互补了加利利链霉菌ATCC31671中缺陷的酮基还原酶基因,使其恢复了产生阿克拉菌酮的能力。4.0kb DNA片段插入方向相反的重组质粒pCBR4在加利利链霉菌ATCC31671中发酵产物经TLC分析证明也是阿克拉菌酮,这说明4.0kbDNA片段中麦迪霉素产生菌酮基还原酶基因具有自身的启动子。对4.0kb DNA片段进行了限制酶酶切分析,建立了其酶切图谱。以actⅢ基因为探针,经分子杂交以及亚克隆和DNA转化实验,将麦迪霉素产生菌酮基还原酶基因定位于BssHⅡ-BamHⅠ1.3kb DNA片段上。对1.3kb DNA片段核苷酸序列分析结果表明:此1.3kb DNA片段中含有一个独...

将麦迪霉素产生菌基因文库中与放线紫红素酮基还原酶基因actⅢ有同源性的4.0kb DNA片段克隆到质粒载体pWHM3中,构成重组质粒pCB4。将质粒pCB4转入酮基还原酶基因缺陷菌株——加利利链霉菌ATCC31671中,得到转化子。转化子发酵产物经TLC和HPLC分析证明是阿克拉菌酮,与加利利链霉菌原株ATCC31133的产物相同,说明麦迪霉素产生菌酮基还原酶基因互补了加利利链霉菌ATCC31671中缺陷的酮基还原酶基因,使其恢复了产生阿克拉菌酮的能力。4.0kb DNA片段插入方向相反的重组质粒pCBR4在加利利链霉菌ATCC31671中发酵产物经TLC分析证明也是阿克拉菌酮,这说明4.0kbDNA片段中麦迪霉素产生菌酮基还原酶基因具有自身的启动子。对4.0kb DNA片段进行了限制酶酶切分析,建立了其酶切图谱。以actⅢ基因为探针,经分子杂交以及亚克隆和DNA转化实验,将麦迪霉素产生菌酮基还原酶基因定位于BssHⅡ-BamHⅠ1.3kb DNA片段上。对1.3kb DNA片段核苷酸序列分析结果表明:此1.3kb DNA片段中含有一个独立的ORF,起始密码ATG,终止密码TAG,含783bp;在起始密码上游有GGAGG5个核苷酸SD序列;此ORF编码260个氨基酸,与actⅢ基因编码的261个氨基酸相似性为77.4%,相同性为66.7%,对麦迪霉素产生菌酮基还原酶基因的可能作用进行了讨论。

NADPH dependent acetoacetyl CoA reductase gene (phbB) and poly β hydroxybutyrate (PHB) synthase gene (phbC) for biosynthesis of PHB were amplified and cloned from chromosomal DNA of Alcaligenes eutrophus H16 using PCR. The restriction maps and sequencing results show that both phbB and phbC have been cloned. It was found that the two genes cloned were highly homologous in DNA sequences to those being reported abroad. By DNA processing, the authors have constructed three tuber specific plant expression vectors:...

NADPH dependent acetoacetyl CoA reductase gene (phbB) and poly β hydroxybutyrate (PHB) synthase gene (phbC) for biosynthesis of PHB were amplified and cloned from chromosomal DNA of Alcaligenes eutrophus H16 using PCR. The restriction maps and sequencing results show that both phbB and phbC have been cloned. It was found that the two genes cloned were highly homologous in DNA sequences to those being reported abroad. By DNA processing, the authors have constructed three tuber specific plant expression vectors: pPSAGB (containing phbB), pBIBGC (containing phbC) and pPSAGCB (containing both phbB and phbC).

利用聚合酶链式反应(PCR)技术,从真养产碱杆菌Alcaligenes eutrophus H16 染色体DNA 中扩增并克隆了调控聚-β-羟基丁酸(poly-β-hydroxybutyrate, PHB)生物合成的两个关键酶基因:依赖NADPH 的乙酰乙酰CoA 还原酶基因(phbB)和PHB合成酶基因(phbC)。限制性内切酶图谱和核苷酸序列分析证实了克隆结果,并表明所克隆的基因与国外报道的有很高的同源性。经过基因拼接,构建了块茎特异性表达的高等植物表达载体pPSAGB(嵌合phbB)、pBIBGC(嵌合phbC)和pPSAGCB(嵌合phbB和phbC双基因)

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关还原酶基因的内容
在知识搜索中查有关还原酶基因的内容
在数字搜索中查有关还原酶基因的内容
在概念知识元中查有关还原酶基因的内容
在学术趋势中查有关还原酶基因的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社